Becerril PDE, Rodríguez LLG, Jasso OJC, Vega MME, Saeb LM

Language: Spanish
References: 27
Page: 271-275
PDF size: 174.38 Kb.

ABSTRACT

Sinus histiocytosis with massive lymphadenopathy, or Rosai- Dorfman disease is a non Langerhans cell histiocytosis. Similar to dermal Langerhans cells; express the histiocyte marker S100. This disease presents massive lymphadenopathy with extraganglionar affection, being the skin the most frequent site, followed by the paranasal sinuses. It is more common in young women, but can also occur in children. The physiopathology is unknown; however it has been associated with autoimmune diseases. For this reason it has been proposed there is an underlying abnormality alteration in cellular immunity. The most important histopathological feature for the diagnosis is emperipolesis. Spontaneous remissions can be achieved; and the first line treatment are corticosteroids, but chemotherapy and radiotherapy have been used with an appropriate response. We present a 39 years old woman with Rosai-Dorfman disease associated with an interstitial granuloma annulare. This association had been previously reported just twice in the literature.

REFERENCES

1. Foucar E, Rosai J, Dorfman R. “Sinus histicyitosis with massive lymphadenopathy. A newly recognized benign clinic pathological entity (Rosai- Dorfman Disease)”. Semin Diagn Pathol. 1990; 7: 19-73.

2. Ortiz HC, Cuesta MT, Ochoa OC, Valenzuela EA, Toussaint CS. “Enfermedad de Rosai-Dorfman, limitada a la piel, informe de cuatro casos”. Gac Méd Méx. 2003; 139: 1-6.

3. Brenn T, Colanje E, Granter S, Leonard N, Grayson W, Fletcher C, et al. “Cutaneous Rosai-Dorfman is a Distinct Clinical Entity”. J Am Acad Dermatol. 2002; 24: 385-391.

4. Quezada PE, Escobar GG, Castrejon VM, Vargas CM, Guido BR. Gorraez de la Mora M. et al. “Enfermedad de Rosai-Dorfman (histiocitosis sinusoidal con linfadenopatía masiva): comunicación de un caso y revisión de la bibliografía”. Revista Alergia México. 2008, 55 (5): 206-211

5. Van ZJ. “Cutaneous Rosai-Dorfman disease”. Dermatology Online Journal. 2004; 10: 12.

6. Bist SS, Vasrhney S, Bisht M, Pathak VP, Kusum A, Gupta N. “Rosai- Dorfman Syndrome – A rare Clinical Entity. Indian J. Otolaryngol”. Head Neck Surg. 2007, 59:184-186.

7. Goodman WT, Barrett TL “Histiocytoses”. En: Bolognia J, Jorizzo J, Rapini R. Dermatology. 2a ed. Madrid, Elsevier, 2008. 1395-1410.

8. Navarrete FG, Novales J, Jurado SF, Medina CD, Lópezportillo SL, Mendoza AL. “Histicitosis Sinusal Cutánea. Estudio Clínico-Patológico”. Dermatología Rev Mex. 2001; 45(4): 173-179

9. Marie I, Verdier E, Courville P, Manrique A, Ducastelle T, Joly P, et al. “Rosai-Dorfman Disease and Granuloma Annulare”. Acta Derm Venereol, 2007; 87: 375-377.

10. Fang KS, Lawry M, Haas A. “Papules on the hands. Granuloma annulare”. Arch Dermatol. 2001; 137 (12): 1647-1652.

11. Howard A, White CR. “Non-infectious Granulomas”. En: Bolognia J, Jorizzo J, Rapini R. Dermatology. 2a ed. Madrid, Elsevier, 2008. 1421-1435.

12. García FM, Curcó BN, Pagerols BX, Vives PV. “Granuloma anular maculoso. Siete nuevos casos”. Med Cutan Iber Lat Am 2004; 32(1): 23-26

13. Victor CF, Mengden S. “Granuloma annulare, patch type”. Dermatology Online Journal. 2008; 14 (5): 21.

14. Fayyazi A, Schweyer S, Eichmeyer B, Herms J, Hemmerlein B, Radzun HJ, Berger H. “Expression of IFNγ, coexpression of TNFα and matrix metalloproteinases and apoptosis of T lymphocytes and macrophages in granuloma annulare”. Arch Dermatol Res. 2000; 292 (8): 384–390.

15. Friedman-Birnbaum R, Weltfriend S, Munichor M, Lichtig C. “A comparative histopathologic study of generalized and localized granuloma annulare”. Am J Dermatopathol 1989; 11: 144-148.

16. Calonje JE, Brenn T, Lazar A. “Granulomatous, necrobiotic and Perforating dermatoses”. En: McKees´s Pathology of the Skin with Clinical Correlations. 4th ed. China. Elsevier, 2012. 288-294.

17. Tsuruta D, Sowa J, Hiroyasu S, Ishii M, Kobayashi H. “Concomitant occurrence of patch granuloma annulare and classical granuloma annulare”. Journal of Dermatology, 2011; 38: 482–485.

18. Mutasim DF. Bridges AG. “Patch Granuloma Annulare: Clinicopathologic study of 6 patients”. J Am Acad Dermatol. 2000; 42: 417-421.

19. Jeff DH, Raymond LB. “Nodular and Diffuse Cutaneous Infiltrates”. En: Dermatopathology, 3a ed. New York, Mc Graw Hill Medical, 2010. 98-135.

20. Scheel MM, Rady PL, Tyring SK, Pandya AG. “Sinus histiocytosis with massive lymphadenopathy: Presentation as giant granuloma annulare and detection of human herpesvirus 6”. J Am Acad Dermatol. 1997; 37: 643-646.

21. Toro JR, Chu P, Yen TS, Leboit PE. “Granuloma annulare and human immunodeficiency virus infection”. Arch Dermatol. 1999; 135: 1341–1346.

22. Henter JI, Tondini C, Pritchard J. “Histiocyte disorders”. Crit Rev Oncol Hematol. 2004; 50: 157–174.

23. Stefanato CM, Ellerin PS, Bhawan J. “Cutaneous sinus histiocytosis (Rosai-Dorfman disease) presenting clinically as vasculitis”. J Am Acad Dermatol. 2002; 46: 775–778.

24. Levine PH, Jahan N, Murari P, Manak M, Jaffe ES. Detection of human herpes virus 6 in tissues involved by sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease). J Infect Dis 1992; 166: 291–295

25. Sita G, Guffanti A, Colombi M, Ferrari A, Neri A, Baldini L. “Rosai-Dorfman syndrome with extranodal localizations and response to glucocorticoids: a case report”. Haematologica. 1996; 81: 165-167.

26. McClain KL, Natkunam Y, Swerdlow SH. “Atypical cellular disorders”. Hematology. 2004; 283-296.

27. Aouba A, Terrier B, Vasiliu V, Candon S, Brousse N, Varet B, et al. “Dramatic clnical efficacy of cladribine in Rosai-Dorfman disease an evolution of the cytokine profile: towards a new therapeutic approach”. Haematologica. 2006, 91 (11): 144-145.